RET, ret proto-oncogene, 5979

N. diseases: 607; N. variants: 162
Disease: Familial medullary thyroid carcinoma ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs377767395
rs377767395
Entrez Id: 5979
Gene Symbol: RET
RET
CUI: C1833921
Disease:
Familial medullary thyroid carcinoma 		0.010 GeneticVariation BEFREE The phenotype of families with Y606C or L790F mutation was categorized as familial medullary thyroid carcinoma. 26254625 2016